JPS63164841A - Production of lactic acid fermentation product - Google Patents

Production of lactic acid fermentation product

Info

Publication number
JPS63164841A
JPS63164841A JP30934586A JP30934586A JPS63164841A JP S63164841 A JPS63164841 A JP S63164841A JP 30934586 A JP30934586 A JP 30934586A JP 30934586 A JP30934586 A JP 30934586A JP S63164841 A JPS63164841 A JP S63164841A
Authority
JP
Japan
Prior art keywords
lactic acid
milk
proteins
acid fermentation
protein
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP30934586A
Other languages
Japanese (ja)
Other versions
JPH0640796B2 (en
Inventor
Yumiko Fujita
藤田 有見子
Takaaki Matsuo
高明 松尾
Ryosuke Momen
良介 木綿
Minoru Kimoto
実 木本
Yukio Hashimoto
征雄 橋本
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fuji Oil Co Ltd
Original Assignee
Fuji Oil Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Fuji Oil Co Ltd filed Critical Fuji Oil Co Ltd
Priority to JP61309345A priority Critical patent/JPH0640796B2/en
Publication of JPS63164841A publication Critical patent/JPS63164841A/en
Publication of JPH0640796B2 publication Critical patent/JPH0640796B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To produce a lactic acid fermentation product having excellent flavor in a short time, by adding a specific oligopeptide blend to a milk component- containing raw material to carry out lactic acid fermentation. CONSTITUTION:Proteins, e.g. egg white, are enzymically hydrolyzed in the coexistence of an endo type protease and exo type protease in an aqueous system for 0.5-10hr to provide (B) an oligopeptide blend having 2-15 average chain length derived from the proteins other than milk component-containing proteins. 0.05-10pts.wt. component (B) (dried material) is then added to (A) 100pts.wt. milk component-containing raw material, e.g. cow's milk, and the resultant blend is homogenized. Lactic acid bacteria are then added to carry out lactic acid fermentation.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は乳酸醗酵物を短時間に製造(乳酸醗酵促進)で
きる方法を提供するものである。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Field of Application) The present invention provides a method for producing a lactic acid fermentation product in a short time (promoting lactic acid fermentation).

(従来技術) 従来から乳酸醗酵の促進剤としてアミノ糖(特公昭45
−3189 ) 、特定動物肉の酵素分解低分子ペプチ
ド(特公昭56〜5134 ’) 、麦芽エキスとホエ
ー蛋白氷解物の併用(特開昭59−220153 )、
蛋白原料の氷解物を醤油乳酸菌処理する方法(特公昭5
5−39308.同51−36340等)等が知られて
いる。しかし、アミノ糖は煩雑な処理を必要とし、特定
動物肉は大量入手が困難であり実用的でない。本願は醤
油等のようにオリゴペプチド自体を乳酸醗酵するもので
はなく、乳成分含有原料に添加して乳成分含有原料の乳
酸醗酵を促進するものである。
(Prior art) Amino sugars (Special Publications in 1973) have traditionally been used as promoters of lactic acid fermentation.
-3189), enzymatically decomposed low-molecular-weight peptides of specific animal meat (Japanese Patent Publication No. 56-5134'), combination of malt extract and whey protein thawed product (Japanese Patent Publication No. 59-220153),
Method for treating melted protein raw material with soy sauce lactic acid bacteria
5-39308. 51-36340, etc.) are known. However, amino sugars require complicated processing, and specified animal meat is difficult to obtain in large quantities, making it impractical. In the present application, the oligopeptide itself is not subjected to lactic acid fermentation like soy sauce, etc., but is added to a milk component-containing raw material to promote lactic acid fermentation of the milk component-containing raw material.

(解決しようとする問題点) 本発明者等は乳成分含有原料の乳酸醗酵促進を目的とし
た。より好ましくは出来るだけ入手容易な原料を用い、
風味の優れた短時間乳酸醗酵促進を目的とした。
(Problems to be Solved) The present inventors aimed to promote lactic acid fermentation of raw materials containing milk components. More preferably, using raw materials that are as easily available as possible,
The purpose was to promote short-term lactic acid fermentation with excellent flavor.

(問題を解決する為の手段) 本発明者等は前記目的を達成すべく種々の蛋白、その氷
解物を検討するなかで、カゼイン等の乳成分蛋白及びそ
の氷解物は乳酸醗酵促進効果が極めて少ないのに、これ
ら乳成分に含まれる蛋白以外の蛋白の氷解物、例えば卵
白又は大豆蛋白等の油糧種子蛋白等の氷解物のうち特定
鎖長の範囲のものが、乳成分含有原料の乳酸醗酵促進効
果を有することを見出し本発明を完成するに到った。
(Means for Solving the Problem) In order to achieve the above object, the present inventors investigated various proteins and their melted products, and found that milk component proteins such as casein and their melted products have an extremely effective lactic acid fermentation promoting effect. Although it is small, melted products of proteins other than proteins contained in milk components, such as melted products of oilseed proteins such as egg white or soybean protein, with a specific chain length range, are lactic acid of milk component-containing raw materials. They discovered that it has a fermentation promoting effect and completed the present invention.

即ち、本発明は乳成分含有原料に対し乳成分含有蛋白以
外の蛋白由来の平均鎖長15以下のオリゴペプチド混合
物を加え、乳酸醗酵することを特徴とする乳酸醗酵物の
製造法である。
That is, the present invention is a method for producing a lactic acid fermented product, which is characterized in that a mixture of oligopeptides having an average chain length of 15 or less derived from proteins other than milk component proteins is added to a milk component-containing raw material, and the mixture is subjected to lactic acid fermentation.

本発明の乳成分含有原料は乳成分の少なくとも一つ以上
を含むことが必要である。例えば、カゼイン、ラクトア
ルブミン、乳糖、ホエー、脱脂粉乳等を含むことが必要
である。又、これらの成分の酵素氷解物を含んでもよい
。例えば、カゼイン、ラクトアルブミン成分の一部又は
全部をこれらの酵素氷解物(分子量は平均鎖長2以上で
あれば特に限定しない)とすることは妨げない。前記乳
成分と本願のオリゴペプチド混合物との組合せにより乳
酸醗酵促進効果がある。
The milk component-containing raw material of the present invention needs to contain at least one milk component. For example, it is necessary to contain casein, lactalbumin, lactose, whey, skim milk powder, etc. It may also contain enzymatically decomposed products of these components. For example, part or all of the casein and lactalbumin components may be decomposed by these enzymes (the molecular weight is not particularly limited as long as the average chain length is 2 or more). The combination of the milk component and the oligopeptide mixture of the present invention has the effect of promoting lactic acid fermentation.

本発明に用いるオリゴペプチド混合物は乳成分含有蛋白
以外の蛋白由来の平均鎖長15以下(2〜15)のオリ
ゴペプチド混合物が適当である。カゼインやラクトアル
ブミン等の乳成分含有蛋白由来のオリゴペプチド混合物
は乳酸醗酵促進効果が極めて少ない。通常、卵白、大豆
蛋白等の油糧種子蛋白が入手が容易なうえに、蛋白含量
も高く工業レベルで実用容易であり好ましい。特殊な蛋
白は大量入手が困難なばかりでなく、工業的に安価に大
量生産が困難であり産業上のメリットがない。
The oligopeptide mixture used in the present invention is suitably a mixture of oligopeptides derived from proteins other than milk-containing proteins and having an average chain length of 15 or less (2 to 15). Oligopeptide mixtures derived from milk-containing proteins such as casein and lactalbumin have extremely little effect on promoting lactic acid fermentation. Usually, oilseed proteins such as egg white and soybean protein are preferred because they are easily available, have a high protein content, and are easy to put into practical use at an industrial level. Special proteins are not only difficult to obtain in large quantities, but also difficult to mass-produce at low cost, and therefore have no industrial advantage.

例えば、特殊なシカ科動物骨格筋等の入手容易でない動
物由来の蛋白は実用的でなく不適である。
For example, proteins derived from animals that are not easily available, such as special cervid skeletal muscles, are impractical and inappropriate.

又、麦芽等は、従来からエキスとして各種醗酵に用いら
れているものの、蛋白含量が少なく、本発明のオリゴペ
プチド混合物原料として実用的でなく不通である。
Furthermore, although malt has been conventionally used as an extract in various fermentations, it has a low protein content and is therefore impractical and unusable as a raw material for the oligopeptide mixture of the present invention.

本発明に用いるオリゴペプチド混合物の平均鎖長が15
を越えると乳酸醗酵促進効果が減少する。
The average chain length of the oligopeptide mixture used in the present invention is 15
If it exceeds this, the lactic acid fermentation promoting effect will decrease.

又、平均鎖長が短くアミノ酸程度では、乳酸醗酵促進効
果が減少するばかりか、得られる乳酸醗酵物がアミノ酸
特有の嫌な風味がして好ましくない。
Furthermore, if the average chain length is short and is comparable to that of an amino acid, not only will the lactic acid fermentation promoting effect be reduced, but the obtained lactic acid fermented product will have an unpleasant flavor peculiar to amino acids, which is not desirable.

通常平均鎖長2以上が適当である。又、遊離アミノ酸が
25%を越えると、乳酸醗酵促進効果が減少したり、ア
ミノ酸特有の嫌な風味が発生することがある。
Usually, an average chain length of 2 or more is appropriate. Furthermore, if the free amino acid content exceeds 25%, the lactic acid fermentation promoting effect may decrease or an unpleasant flavor peculiar to amino acids may occur.

オリゴペプチド混合物の製造態様は蛋白を公知の方法に
よりプロテアーゼを用いて水系下に水解して得ることが
できるが、通常苦味が発生することが多く、好ましくは
、特願昭60−281685等に開示されるように蛋白
を、エンド型プロテアーゼ及びエキソ型プロテアーゼ共
存水系下に、0.5〜10時間酵素分解して苦味のない
風味の優れたオリゴペプチド混合物を得ることが適当で
ある。
The oligopeptide mixture can be produced by hydrolyzing proteins in an aqueous system using protease using a known method, but this usually produces a bitter taste, so it is preferable to use the method disclosed in Japanese Patent Application No. 60-281685. It is appropriate to enzymatically decompose proteins for 0.5 to 10 hours in an aqueous system coexisting with endo-type protease and exo-type protease to obtain an oligopeptide mixture with no bitterness and excellent flavor.

本発明において、平均鎖長15以下のオリゴペプチド混
合物(乾燥物として)を乳成分含有原料100重量部に
対し0.05〜10重量部、好ましくは0.1〜5重量
部加え、乳酸醗酵することが適当である。
In the present invention, 0.05 to 10 parts by weight, preferably 0.1 to 5 parts by weight, of an oligopeptide mixture (as a dry product) having an average chain length of 15 or less is added to 100 parts by weight of the milk-containing raw material, and lactic acid fermentation is carried out. That is appropriate.

0.05重量部未満では乳酸醗酵促進効果が少なく、1
0重量部を越えても乳酸醗酵促進効果が少なくなる。こ
れは本願に用いるオリゴペプチド混合物の浸透圧に起因
するものと推察される。
If it is less than 0.05 part by weight, the effect of promoting lactic acid fermentation will be small;
Even if it exceeds 0 parts by weight, the effect of promoting lactic acid fermentation will be reduced. This is presumably due to the osmotic pressure of the oligopeptide mixture used in this application.

本発明は乳酸飲料、ヨーグルト、ケフィア、チーズ等の
主に乳酸菌による乳酸醗酵の促進効果がある。例えば、
牛乳を用いたヨーグルトの製造において、目的の酸度に
達するまでに約8時開票するものを、本発明のオリゴペ
プチド混合物添加により約1/2の時間で目的の酸度に
達することができる。又、脱脂粉乳を用いたヨーグルト
の製造において、目的の酸度に達するまでの約5時間要
するものを、本発明のオリゴペプチド混合物添加により
約3.5時間で目的の酸度に達することができる。更に
得られるヨーグルトの風味を改良して美味しいものとす
ることもできる。
The present invention has the effect of promoting lactic acid fermentation mainly by lactic acid bacteria in lactic acid drinks, yogurt, kefir, cheese, etc. for example,
When producing yogurt using milk, it takes about 8 hours to reach the target acidity, but by adding the oligopeptide mixture of the present invention, the target acidity can be reached in about 1/2 the time. Further, in the production of yogurt using skim milk powder, it takes about 5 hours to reach the target acidity, but by adding the oligopeptide mixture of the present invention, the target acidity can be reached in about 3.5 hours. Furthermore, the flavor of the resulting yogurt can be improved to make it more delicious.

以上説明したように、本発明は乳酸醗酵を促進された乳
酸醗酵物のみならず風味的にも優れた乳酸醗酵物を提供
できるものである。又、本発明に用いるオリゴペプチド
混合物を乳酸醗酵のみならず、酵母醗酵、カビ醗酵、そ
の他のバクテリア醗酵若しくはこれらの共存した醗酵に
用いることは妨げない。
As explained above, the present invention can provide not only a lactic acid fermented product with accelerated lactic acid fermentation but also a lactic acid fermented product that is excellent in flavor. Further, the oligopeptide mixture used in the present invention may be used not only for lactic acid fermentation, but also for yeast fermentation, mold fermentation, other bacterial fermentation, or fermentation in which these coexist.

(実施例) 以下実施例により本発明の実施態様を説明する。(Example) Embodiments of the present invention will be described below with reference to Examples.

実験例1 分離大豆蛋白(フジプローR[不二製油n製)100g
の5%水溶液(pH7)をエンド型及びエキソ型プロテ
アーゼ共存するアクチナーゼAs (科研製薬製) I
gを用いて50℃で5時間酵素分解し、p1)7に再調
整後70℃で30分間加熱して酵素失活させ、5000
rpm X 20分間遠心分離して得た上澄みを噴霧乾
燥して大豆オリゴペプチド混合物を得た。 尚、平均鎖
長は特開昭60−281685記載の方法を用いて測定
した結果7.7(尚、遊離アミノ酸含量は18%)であ
った。
Experimental Example 1 Isolated soybean protein (Fujipro R [manufactured by Fuji Oil Co., Ltd.] 100g)
A 5% aqueous solution (pH 7) of Actinase As (manufactured by Kaken Pharmaceutical Co., Ltd.) containing endo-type and exo-type proteases I
Enzymatically decompose the enzyme at 50°C for 5 hours using p1), then heat it at 70°C for 30 minutes to inactivate the enzyme, and then
The supernatant obtained by centrifugation at rpm x 20 minutes was spray-dried to obtain a soybean oligopeptide mixture. The average chain length was measured using the method described in JP-A-60-281685 and was found to be 7.7 (free amino acid content was 18%).

実施例1 牛乳Loom 1に脱脂粉乳4.8g及び実施例1で得
られた大豆オリゴペプチド混合物0.2gを加えた混合
液を50〜60℃に加熱し、ホモゲナイザーを用いて1
50kg /−にて均質化し、80〜90℃にて10分
間加熱し、後42℃まで冷却し、カルチャースターター
(Lactobacillus bulgaricus
及びStreptococcusthermophi 
1lusの混合スターターを牛乳培地で17時間培養し
た酸度1.菌数9×10の8乗f[M/mj?)1ml
を添加し、42℃で乳酸醗酵を行い、酸度、菌数の経時
的変化をみた。結果を第1図に示す。
Example 1 A mixture of Milk Loom 1, 4.8 g of skimmed milk powder, and 0.2 g of the soybean oligopeptide mixture obtained in Example 1 was heated to 50 to 60°C, and then mixed using a homogenizer to
Homogenized at 50 kg/-, heated at 80-90°C for 10 minutes, then cooled to 42°C, culture starter (Lactobacillus bulgaricus)
and Streptococcus thermophi
Acidity: 1.1 lus of mixed starter was cultured in milk medium for 17 hours. Number of bacteria 9 x 10 to the 8th power f [M/mj? ) 1ml
was added to carry out lactic acid fermentation at 42°C, and changes in acidity and bacterial count over time were observed. The results are shown in Figure 1.

尚、コントロールは該ペプチドの代わりに脱脂粉乳5.
0gを用いた。
As a control, skim milk powder 5. was used instead of the peptide.
0g was used.

第1図から明らかなようにヨーグルトの完成である酸度
0.8に達するまでに、コントロールは5時間かかった
ものを、大豆オリゴペプチド混合物を加えたものは3.
5時間しかかからなかった。
As is clear from Figure 1, the control took 5 hours to reach the acidity level of 0.8, which is the final level of yogurt, while the yogurt to which the soybean oligopeptide mixture was added took 3 hours.
It only took 5 hours.

又、得られたヨーグルトもコントロールより美味しいも
のであった。
Moreover, the obtained yogurt was also more delicious than the control.

実験例2 卵白を用い実験例Iと同様にして平均鎖長5.3、遊離
アミノ酸15%の卵白オリゴペプチド混合物を得た。
Experimental Example 2 Using egg white, an egg white oligopeptide mixture having an average chain length of 5.3 and 15% of free amino acids was obtained in the same manner as in Experimental Example I.

実施例2 実験例1で得られた卵白オリゴペプチド混合物を実施例
1の大豆オリゴペプチド混合物の代わりに用い、実施例
1と同様にしてヨーグルトを製造した。
Example 2 Yogurt was produced in the same manner as in Example 1, using the egg white oligopeptide mixture obtained in Experimental Example 1 instead of the soybean oligopeptide mixture in Example 1.

酸度が0.8に達する時間は実施例1の大豆オリゴペプ
チド混合物のときと同様3.5時間で、風味のよいヨー
グルトが得られた。
The time required for the acidity to reach 0.8 was 3.5 hours, the same as in the case of the soybean oligopeptide mixture in Example 1, and a yogurt with good flavor was obtained.

実験例3 実験例1と同様にして市販カゼインを水解して平均鎖長
5.4、遊離アミノ酸13.3%ののカゼインオリゴペ
プチド混合物を得た。
Experimental Example 3 Commercially available casein was hydrolyzed in the same manner as in Experimental Example 1 to obtain a casein oligopeptide mixture with an average chain length of 5.4 and a free amino acid content of 13.3%.

比較例1 実験例3で得られたカゼインオリゴペプチド混合物を大
豆オリゴペプチド混合物の代わりに用い、実施例1と同
様にしてヨーグルトを得た。
Comparative Example 1 Yogurt was obtained in the same manner as in Example 1, using the casein oligopeptide mixture obtained in Experimental Example 3 instead of the soybean oligopeptide mixture.

酸度が0.8に達する時間は5時間で、乳酸醗酵促進効
果は認められなかった。
It took 5 hours for the acidity to reach 0.8, and no lactic acid fermentation promoting effect was observed.

比較例2 アミノ酸組成物(平均鎖長1.0、アミノ酸組成は大豆
オリゴペプチド混合物のそれと同一組成になるように調
製した)、分離大豆蛋白(不二製油■製フジブローR(
未水解))を実施例1の大豆蛋白ペプチド混合物の代わ
りに用い、実施例1と同様にしてヨーグルトを製造した
。酸度0.8に達するまでの醗酵時間及び風味は、アミ
ノ酸組成物の場合5.0時間かかり、アミノ酸特有の嫌
な味がし、大豆蛋白の場合5時間かかり、風味的には好
適のものであった。
Comparative Example 2 Amino acid composition (average chain length 1.0, amino acid composition was prepared to be the same as that of the soybean oligopeptide mixture), isolated soybean protein (Fujiburo R manufactured by Fuji Oil ■),
Yogurt was produced in the same manner as in Example 1, using the unhydrolyzed (non-hydrolyzed)) in place of the soybean protein peptide mixture of Example 1. Regarding the fermentation time and flavor to reach acidity of 0.8, it takes 5.0 hours for the amino acid composition, which has an unpleasant taste peculiar to amino acids, and it takes 5 hours for soybean protein, which is not suitable in terms of flavor. there were.

実施例3 実験例Iと同様にして得た大豆ペプチド混合物の添加量
を表−1のように変えて、実施例1と同様にしてヨーグ
ルトを得た。酸度が0.8に達するまでの時間を併せ表
−1に示す。
Example 3 Yogurt was obtained in the same manner as in Example 1, except that the amount of the soybean peptide mixture obtained in the same manner as in Experimental Example I was changed as shown in Table-1. The time required for the acidity to reach 0.8 is also shown in Table 1.

(以下余白) 表−1 添加割合(g )   醗酵時間(Hr)05.0 0.05       4.5 0.2       3.5 1.0       3.2 5.0      、 3.8 1).0       6.0  ゲル化せず実験例4 分離大豆蛋白10%水溶液(pH7,0) 2kgをプ
ロチン−AC(大和化成側製> 200mgを用いて、
50℃で5〜10時間水解し、pH7に再調整後70℃
で30分間加熱して酵素失活させ、5000RPMで遠
心分離して上澄みを得、凍結乾燥して、■平均鎖長6.
8、遊離アミノrv10.5%の大豆オリゴペプチド混
合物、■平均鎖長17.0、遊離アミノ酸0.5%の大
豆オリゴペプチド混合物を得た。
(Margin below) Table-1 Addition ratio (g) Fermentation time (Hr) 05.0 0.05 4.5 0.2 3.5 1.0 3.2 5.0, 3.8 1). 0 6.0 No gelation Experimental Example 4 2 kg of 10% isolated soy protein aqueous solution (pH 7,0) was mixed with Protin-AC (manufactured by Daiwa Kasei > 200 mg).
Hydrolyzed at 50℃ for 5 to 10 hours, readjusted to pH 7, then 70℃
The enzyme was inactivated by heating for 30 minutes at 5,000 RPM, and the supernatant was obtained by centrifugation at 5,000 RPM.
8. A soybean oligopeptide mixture with a free amino rv of 10.5%, (2) A soybean oligopeptide mixture with an average chain length of 17.0 and a free amino acid content of 0.5%.

実施例4 実験例4で得られた大豆オリゴペプチド混合物を用い、
実施例1と同様にしてヨーグルトを得た。
Example 4 Using the soybean oligopeptide mixture obtained in Experimental Example 4,
Yogurt was obtained in the same manner as in Example 1.

■平均鎖長6.8、遊離アミノ酸0.5%の大豆オリゴ
ペプチド混合物の場合、酸度0.8に達するのに4.0
時間要し、■平均鎖長17.0、遊離アミノ酸0゜5%
の大豆オリゴペプチド混合物場合、酸度0.8に達する
のに5.0時間要した。各々、若干苦い風味を呈した。
■In the case of a soybean oligopeptide mixture with an average chain length of 6.8 and 0.5% free amino acids, it takes 4.0% to reach an acidity of 0.8.
Time required, ■Average chain length 17.0, free amino acids 0°5%
In the case of the soybean oligopeptide mixture, it took 5.0 hours to reach an acidity of 0.8. Each exhibited a slightly bitter flavor.

(効果) 以上説明したように、本発明により、ヨーグルト、チー
ズ等の乳#J、醗酵に際し、乳酸醗酵の時間を短縮(乳
酸醗酵促進)することが可能になったものである。
(Effects) As explained above, the present invention makes it possible to shorten the lactic acid fermentation time (promote lactic acid fermentation) when fermenting milk #J such as yogurt and cheese.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は牛乳−脱脂粉乳水溶液の乳酸醗酵の酸度と時間
の関係を表す図面であり、・−・は大豆オリゴペプチド
混合物添加、〇−・−・−〇は無添加を表す。 手続補正書(方式) %式% 1、事件の表示 昭和61年特許願第309345号 2、発明の名称 乳酸醗酵物の製造法 3、補正をする者 事件との関係  特許出願人 住 所 大阪市南区へ幡町6番1 名 称 不二製油株式会社 代表者 久 本 浩一部 4、代理人 住所 大阪市淀用区東三国1丁目32番12号5、補正
命令の日付(発送日) 62、5,13 : 、、−、、、、−+−。 久ス 7、補正の内容
FIG. 1 is a diagram showing the relationship between acidity and time in lactic acid fermentation of a milk-skim milk powder aqueous solution, where . . . represents the addition of a soybean oligopeptide mixture, and 〇-.--.-〇 represents no addition. Procedural amendment (method) % formula % 1. Indication of the case Patent Application No. 309345 of 1985 2. Name of the invention Method for producing lactic acid fermented products 3. Person making the amendment Relationship with the case Patent applicant address Osaka City 6-1 Hatamachi to Minami-ku Name Fuji Oil Co., Ltd. Representative Hiroshi Hisamoto 4, Agent address 1-32-12-5 Higashi Mikuni, Yodoyo-ku, Osaka City Date of amendment order (shipment date) 62 ,5,13: ,,-,,,,-+-. Kusu 7, Contents of correction

Claims (5)

【特許請求の範囲】[Claims] (1)乳成分含有原料に対し乳成分含有蛋白以外の蛋白
由来の平均鎖長15以下のオリゴペプチド混合物を加え
、乳酸醗酵することを特徴とする乳酸醗酵物の製造法。
(1) A method for producing a lactic acid fermented product, which comprises adding a mixture of oligopeptides having an average chain length of 15 or less derived from proteins other than milk-containing proteins to a milk-containing raw material and carrying out lactic acid fermentation.
(2)乳成分含有原料100重量部に対し乳成分含有蛋
白以外の蛋白由来の平均鎖長15以下のオリゴペプチド
混合物を0.05重量部〜10重量部加え、乳酸醗酵す
る特許請求の範囲第(1)項記載の製造法。
(2) 0.05 to 10 parts by weight of an oligopeptide mixture with an average chain length of 15 or less derived from a protein other than milk-containing protein is added to 100 parts by weight of the milk-containing raw material, and lactic acid fermentation is carried out. The manufacturing method described in (1).
(3)乳成分含有蛋白以外の蛋白が卵白又は大豆蛋白等
の油糧種子蛋白である特許請求の範囲第(1)項記載の
製造法。
(3) The production method according to claim (1), wherein the protein other than the milk-containing protein is an oilseed protein such as egg white or soybean protein.
(4)オリゴペプチド混合物の遊離アミノ酸が25%以
下である特許請求の範囲第(1)項記載の製造法。
(4) The production method according to claim (1), wherein the free amino acid content of the oligopeptide mixture is 25% or less.
(5)オリゴペプチド混合物が、乳成分含有蛋白以外の
蛋白を、エンド型プロテアーゼ及びエキソ型プロテアー
ゼ共存水系下に、0.5〜10時間酵素分解して得られ
る、苦味の極めて少ないオリゴペプチド混合物である特
許請求の範囲第(1)項記載の製造法。
(5) The oligopeptide mixture is an oligopeptide mixture with extremely low bitterness obtained by enzymatically decomposing proteins other than milk-containing proteins in an aqueous system coexisting with endo-type proteases and exo-type proteases for 0.5 to 10 hours. A manufacturing method according to claim (1).
JP61309345A 1986-12-26 1986-12-26 Lactic acid fermented product manufacturing method Expired - Fee Related JPH0640796B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61309345A JPH0640796B2 (en) 1986-12-26 1986-12-26 Lactic acid fermented product manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61309345A JPH0640796B2 (en) 1986-12-26 1986-12-26 Lactic acid fermented product manufacturing method

Publications (2)

Publication Number Publication Date
JPS63164841A true JPS63164841A (en) 1988-07-08
JPH0640796B2 JPH0640796B2 (en) 1994-06-01

Family

ID=17991889

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61309345A Expired - Fee Related JPH0640796B2 (en) 1986-12-26 1986-12-26 Lactic acid fermented product manufacturing method

Country Status (1)

Country Link
JP (1) JPH0640796B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02107153A (en) * 1988-10-14 1990-04-19 Ajinomoto General Foods Inc Coffee whitener
WO2008004794A1 (en) * 2006-07-03 2008-01-10 Sang Kee Han New functional fermented milk (yogurt) for use in dieting
JP2009082010A (en) * 2007-09-27 2009-04-23 Fuji Oil Co Ltd Method for producing fermented food causing little deterioration in product quality

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4954581A (en) * 1972-09-13 1974-05-27
JPS5136340A (en) * 1974-09-18 1976-03-27 Tsuya Wakamatsu SHITAHARANO DEBARIOOSAHERUBYOHARAMAKI
JPS5154976A (en) * 1974-09-05 1976-05-14 Borden Inc BAICHI
JPS5435243A (en) * 1977-08-23 1979-03-15 Nippon Yuukon Kk Quality improver for lactic acid bacillus drink and food
JPS57146546A (en) * 1981-03-06 1982-09-10 Eisai Co Ltd Production of fermented dairy products
JPS59220153A (en) * 1983-05-30 1984-12-11 Kagome Kk Lactic acid fermentation beverage and production thereof

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4954581A (en) * 1972-09-13 1974-05-27
JPS5154976A (en) * 1974-09-05 1976-05-14 Borden Inc BAICHI
JPS5136340A (en) * 1974-09-18 1976-03-27 Tsuya Wakamatsu SHITAHARANO DEBARIOOSAHERUBYOHARAMAKI
JPS5435243A (en) * 1977-08-23 1979-03-15 Nippon Yuukon Kk Quality improver for lactic acid bacillus drink and food
JPS57146546A (en) * 1981-03-06 1982-09-10 Eisai Co Ltd Production of fermented dairy products
JPS59220153A (en) * 1983-05-30 1984-12-11 Kagome Kk Lactic acid fermentation beverage and production thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02107153A (en) * 1988-10-14 1990-04-19 Ajinomoto General Foods Inc Coffee whitener
WO2008004794A1 (en) * 2006-07-03 2008-01-10 Sang Kee Han New functional fermented milk (yogurt) for use in dieting
JP2009082010A (en) * 2007-09-27 2009-04-23 Fuji Oil Co Ltd Method for producing fermented food causing little deterioration in product quality

Also Published As

Publication number Publication date
JPH0640796B2 (en) 1994-06-01

Similar Documents

Publication Publication Date Title
JP4202748B2 (en) Protein hydrolyzate
EP2011402B1 (en) Process for producing stirred whey protein-enriched fermented milk
US5882705A (en) Micellar whey protein, solution thereof, powder thereof, and foods utilizing same
JP2004508025A (en) Improved bioactive whey protein hydrolyzate
EP0711504A1 (en) Process for producing cheese using transglutaminase
JP2683491B2 (en) Whey protein fermented milk and method for producing the same
US6251445B1 (en) Method for producing enzyme-modified cheese flavorings
US6214585B1 (en) Protein hydrolysis
Fox Exogenous enzymes in dairy technology—A review 1
EP1085817B1 (en) Production of cheese flavour
US4699793A (en) Method of producing a seasoning from cheese whey
KR950013948B1 (en) Method of removing bitter taste from hydrolysed protein
JPH07147898A (en) Preparation of fermented soya milk
KR100462424B1 (en) Method for producing yoghurt from soybean residue
JPS63164841A (en) Production of lactic acid fermentation product
CA2468905A1 (en) Cheese flavour ingredient and method of its production
JPH0484855A (en) Production of cheese-flavored composition
JP4307026B2 (en) Lactic acid bacteria growth promoter and process for producing the same
JPS59113869A (en) Formation of cheese flavor having strong taste
JPH0272826A (en) Lactic acid fermented food, production thereof and milk-clotting enzyme
JPH03224448A (en) Production of pure vegerable cheesy food
JPS6291144A (en) Production of fermented whey powder
SU1750603A1 (en) Method of preparing fodder additive
JPH0254061B2 (en)
RU2075941C1 (en) Method of sourly dairy product making

Legal Events

Date Code Title Description
LAPS Cancellation because of no payment of annual fees